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96882-98-3

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96882-98-3 Usage

General Description

(S)-(+)-2-(p-toluenesulfonate)-1,2-propanediol is a chemical compound with the molecular formula C10H14O5S. It is commonly used as a chiral resolving agent in organic synthesis. (S)-(+)-2-(P-TOLUENESULFONATE)-1,2-PROPANEDIOL is an optically pure form of 1,2-propanediol, which is a key intermediate in the synthesis of pharmaceuticals and other fine chemicals. The p-toluenesulfonate group in the compound helps to improve its solubility and reactivity in organic solvents. It is also used as a chiral auxiliary in asymmetric synthesis reactions to control the stereochemistry of the final product. Overall, (S)-(+)-2-(p-toluenesulfonate)-1,2-propanediol is an important compound in the field of organic chemistry due to its usefulness as a resolving agent and chiral auxiliary.

Check Digit Verification of cas no

The CAS Registry Mumber 96882-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96882-98:
(7*9)+(6*6)+(5*8)+(4*8)+(3*2)+(2*9)+(1*8)=203
203 % 10 = 3
So 96882-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4S/c1-8-3-5-10(6-4-8)15(12,13)14-9(2)7-11/h3-6,9,11H,7H2,1-2H3/t9-/m0/s1

96882-98-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S)-1-hydroxypropan-2-yl] 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names (S)-1,2-propanediol 2-tosylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:96882-98-3 SDS

96882-98-3Relevant articles and documents

Enantioselective synthesis of (R)-propylene carbonate from ethyl (S)-lactate

Whitaker, John M.,Ronald, Robert C.

experimental part, p. 1403 - 1404 (2010/02/16)

We report a three-step synthesis of (R)-propylene carbonate from inexpensive, chiral ethyl (S)-lactate. The synthesis involves a borohydride ester reduction and an unusual intramolecular displacement reaction by a carbonate anion. The procedure is simple and reliable, resulting in (R)-propylene carbonate in approximately 60% overall yield with ≥98% ee. Georg Thieme Verlag Stuttgart.

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